Description Usage Arguments Value References Examples
A function that runs BRETIGEA findCells() but returns the used markers
1 | findCellsMod(inputMat, markers, nMarker, method, scale)
|
inputMat |
Numeric gene expression data frame or matrix, with rownames corresponding to gene names, some of which are marker genes, and columns corresponding to samples. |
markers |
Data frame with marker genes in one column (named "marker") and the cell type that that gene symbol corresponds to in another column (named "cell"). |
nMarker |
The number of marker genes (that are present in your expression data set) to use in estimating the surrogate cell type proportion variable for each cell type. |
method |
To estimate the cell type proportions, can either use PCA or SVD. |
scale |
Whether or not to scale the gene expression data from each marker gene prior to using it as an input for dimension reduction. |
Returns a list of sample-by-cell type matrix of estimated cell type proportion variables and the markers used
#' Chikina M, Zaslavsky E, Sealfon SC. CellCODE: a robust latent variable approach to differential expression analysis for heterogeneous cell populations. Bioinformatics . 2015;31(10):1584-91.
Mancarci, B. O., Toker, L., Tripathy, S. J., Li, B., Rocco, B., Sibille, E., & Pavlidis, P. (2017). CrossLaboratory Analysis of Brain Cell Type Transcriptomes with Applications to Interpretation of Bulk Tissue Data. eNeuro, 4(6), ENEURO.0212-17.2017. https://doi.org/10.1523/ENEURO.0212-17.201
R Core Team (2020). R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. URL https://www.R-project.org/.
1 2 3 4 5 6 7 8 9 10 11 12 13 | # Examples 1:
# Using bretCellMarkers, metadata datasets available with package
countDfBret <- countDf
rownames(countDfBret) <- countDfBret$Gene
countDfBret <- countDfBret[,-1]
findCellsModResults <- findCellsMod(
inputMat = countDfBret,
markers = bretCellMarkers,
nMarker = 10,
method = "SVD",
scale = TRUE)
findCellsModResults$markerList
findCellsModResults$SPVS
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